Canonical Allele Identifier: CA383550445
Gene: TNFRSF1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.6442929C>G (hg19) chr12:g.6333763C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6333763C>G , CM000674.2:g.6333763C>G GRCh38
NC_000012.11:g.6442929C>G , CM000674.1:g.6442929C>G GRCh37
NC_000012.10:g.6313190C>G NCBI36
NG_007506.1:g.13333G>C , LRG_193:g.13333G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000366159.9:n.330G>C
ENST00000437813.8:c.296G>C ENSP00000513672.1:p.Cys99Ser
ENST00000440083.7:c.296G>C ENSP00000413224.3:p.Cys99Ser
ENST00000535958.2:c.*123G>C ENSP00000513673.1:n.*123G>C
ENST00000698339.1:c.296G>C ENSP00000513670.1:p.Cys99Ser
ENST00000698340.1:c.296G>C ENSP00000513671.1:p.Cys99Ser
ENST00000162749.7:c.296G>C MANE Select ENSP00000162749.2:p.Cys99Ser
ENST00000162749.6:c.296G>C ENSP00000162749.2:p.Cys99Ser
ENST00000366159.8:c.296G>C ENSP00000380389.3:p.Cys99Ser
ENST00000437813.7:n.257G>C
ENST00000440083.6:c.296G>C ENSP00000413224.2:p.Cys99Ser
ENST00000534885.5:c.142G>C ENSP00000441803.1:p.Ala48Pro
ENST00000535958.1:n.542G>C
ENST00000536194.1:c.269G>C ENSP00000442919.1:p.Cys90Ser
ENST00000539372.5:c.296G>C ENSP00000442059.1:p.Cys99Ser
ENST00000540022.5:c.194-247G>C ENSP00000438343.1:n.194-247G>C
ENST00000543048.5:c.214+82G>C ENSP00000439981.1:n.214+82G>C
ENST00000543995.5:c.194-312G>C ENSP00000442405.1:n.194-312G>C
NM_001065.3:c.296G>C , LRG_193t1:c.296G>C NP_001056.1:p.Cys99Ser
NM_001346091.1:c.-29G>C NP_001333020.1:n.-29G>C
NM_001346092.1:c.-282G>C NP_001333021.1:n.-282G>C
NR_144351.1:n.599G>C
NM_001065.4:c.296G>C MANE Select NP_001056.1:p.Cys99Ser
NM_001346091.2:c.-29G>C NP_001333020.1:n.-29G>C
NM_001346092.2:c.-282G>C NP_001333021.1:n.-282G>C
NR_144351.2:n.558G>C
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